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Biomedical subjects

M Mazloum Ardakani

Publications and source records attributed to M Mazloum Ardakani.

6 recordsLinked to original sources

Thiocyanate ion-selective PVC membrane electrode based on N,N'-ethylene-bis(4-methylsalicylidineiminato)nickel(II).

A highly selective poly(vinyl chloride) (PVC) membrane electrode based on an N,N'-ethylene-bis(4-methyl-salicylidineiminato) nickel(II) [Ni(EBMSI)] complex as a carrier for a thiocyanate-selective electrode is reported. The influences of the membrane composition, pH and possible interfering anions were investigated based on the response properties of the electrode. The electrode exhibited a good Nernstian slope of -58.9 +/- 0.7 mV decade(-1), over a wide pH range of 3.5 - 8.5 and a linear range of 1.0 x 10(-6) - 1.0 x 10(-1) M for thiocyanate. The detection limit of electrode was 3.1 x 10(-7) M SCN(-). The selectivity coefficients determined by a fixed interference method (FIM) indicate that a good discriminating ability towards the SCN- ion compared to other anions. The proposed sensor had a fast response time of about 5 - 15 s and could be used for at least 3 months without any considerable divergence in the potential. It was applied as an indicator electrode in the titration of thiocyanate with Ag+ and in the potentiometric determination of thiocyanate in saliva and urine samples.

Journal Article↗

Sulfate-selective electrode based on a complex of copper.

A new sulfate-selective electrode based on the complex N,N'-bis(2-amino-1-oxo-phenelenyl)phenylenediamine copper(II) (CuL) as the membrane carrier was developed. The electrode exhibited a good Nernstian slope of -29.5 +/- 0.5 mV/decade and a linear range of 1.0 x 10(-7) - 1.0 x 10(-1) M for sulfate. The limit of detection was 1.0 x 10(-8) M. It has a fast response time of 10 s and can be used for more than three months. The selective coefficients were determined by the fixed interference method (FIM). The electrode could be used in the pH range 3.5 - 8.0. It was employed as an indicator electrode for direct determination of sulfate in pharmacy and cement samples.

Journal Article↗

Salicylate poly(vinyl chloride) membrane electrode based on (2-[(E)-2-(4-nitrophenyl) hydrazono]-1-phenyl-2-(2-quinolyl)-1-ethanone) Cu(II).

A new salicylate-selective electrode based on the complex of (2-[(E)-2-(4-nitrophenyl)hydrazono]-1-phenyl-2-(2-quinolyl)-1-ethanone) Cu(II) as the membrane carrier was developed. The electrode exhibited a good Nernstian slope of -59.6+/-1.0 mV/decade and a linear range of 1.0 x 10(-6) to 1.0M for salicylate. The limit of detection was 5.0 x 10(-7) M. The electrode had a fast response time of 10 s and can be used for more than 3 months. The selective coefficients were determined by the fixed interference method and could be used in the pH range of 4.0 to 10.5. The electrode was employed as an indicator electrode for direct determination of salicylate in pharmaceutical and biological samples.

Electrodes↗

Highly selective oxalate-membrane electrode based on 2,2'-[1,4-butandiyle bis(nitrilo propylidine)]bis-1-naphtholato copper(II).

A new oxalate-selective electrode based on the complex 2,2'-[1,4-butandiyle bis(nitrilo propylidine)]bis-1-naphtholato copper(II) (CuL) as the membrane carrier was developed. The electrode exhibited a good Nernstian slope of -29.2+/-0.6 mV/decade (mean value+/-standard deviation, n=5) and a linear range of 5.0 x 10(-8) to 1.0 x 10(-1)M for oxalate. The limit of detection was 5.0 x 10(-8)M. This electrode represents a fast response time (i.e. 10-15s) and could be used for more than 3 months. The selectivity coefficients were determined by the fixed interference method (FIM) and could be used in the pH range of 2.0-7.0. It was employed as an indicator electrode for the determination of oxalate in water samples.

Biosensing Techniques↗

Perchlorate-selective membrane electrode based on a new complex of uranil.

A potentiometric ion-selective electrode based on new compound, as a carrier, has been successfully developed for detection of perchlorate anion in aqueous solution. Within the perchlorate ion concentration range 1.0x10(-6) to 1.0 mol L(-1) the electrode had a linear response with a Nernstian slope of 60.6+/-1.0 mV per decade . The limit of detection as determined from the intersection of the extrapolated linear segments of the calibration plot was 8.0x10(-7) mol L(-1). The proposed electrode has fairly a good discriminating ability towards ClO(4) (-) ion in comparison to other anions. The sensor has a response time of < or =10 s and can be used for at least 2 months without substantial divergence in potential. It was successfully applied to direct determination of perchlorate in urine and water.

Journal Article↗

A copper ion-selective electrode with high selectivity prepared by sol-gel and coated wire techniques.

A sol-gel electrode and a coated wire ion-selective poly(vinyl chloride) membrane, based on thiosemicarbazone as a neutral carrier, were successfully developed for the detection of Cu (II) in aqueous solutions. The sol-gel electrode and coated electrode exhibited linear response with Nernstian slopes of 29.2 and 28.1 mV per decade respectively, within the copper ion concentration ranges 1.0 x 10(-5) - 1.0 x 10(-1) M and 6.0 x 10(-6) - 1.0 x 10(-1) M for coated and sol-gel sensors. The coated and sol-gel electrodes show detection limits of 3.0 x 10(-6) and 6.0 x 10(-6) M respectively. The electrodes exhibited good selectivities for a number of alkali, alkaline earth, transition and heavy metal ions. The proposed electrodes have response times ranging from 10-50 s to achieve a 95% steady potential for Cu2+ concentration. The electrodes are suitable for use in aqueous solutions over a wide pH range (4-7.5). Applications of these electrodes for the determination of copper in real samples, and as an indicator electrode for potentiometric titration of Cu2+ ion using EDTA, are reported. The lifetimes of the electrodes were tested over a period of six months to investigate their stability. No significant change in the performance of the sol-gel electrode was observed over this period, but after two months the coated wire copper-selective electrode exhibited a gradual decrease in the slope. The selectivity of the sol-gel electrode was found to be better than that of the coated wire copper-selective electrode. Based on these results, a novel sol-gel copper-selective electrode is proposed for the determination of copper, and applied to real sample assays.

Journal Article↗